chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117689135117689136TC11GENIChomozygous116080610
7117689911117689912CA38GENIChomozygous115847949
7117690326117690327CA22GENICpossibly homozygous115847951
7117690388117690389TC20GENIChomozygous115847953
7117690825117690826CT37GENIChomozygous116341630
7117691535117691536CA29GENIChomozygous115847955
7117691541117691542CT30GENIChomozygous115847957
7117692538117692539GT27GENIChomozygous115847959
7117692677117692678CT33GENIChomozygous115847961
7117692789117692790AG40GENICpossibly homozygous115847963
7117693000117693001TC38GENIChomozygous115847965
7117693023117693024TG37GENIChomozygous115847967
7117693844117693845GT28GENIChomozygous115847969
7117694013117694014TG41GENIChomozygous115847971
7117694816117694817TC30GENIChomozygous115847973
7117696183117696184AG28GENIChomozygous115847975
7117697243117697244AG41GENIChomozygous115847977
7117697852117697853GC32GENIChomozygous115847979
7117698209117698210CT35GENIChomozygous115847981
7117698224117698225GA39GENIChomozygous115847983
7117698957117698958AG29GENIChomozygous115847987
7117699260117699261GA16GENIChomozygous116341632
7117699268117699269CA16GENIChomozygous116341634
7117699270117699271CA17GENIChomozygous116341636
7117702547117702548TC34GENIChomozygous116302250